Zobrazeno 1 - 10
of 171
pro vyhledávání: '"Zhixian Yang"'
Autor:
Huaizhi Zong, Zhixian Yang, Xiu Yu, Junhui Zhang, Jikun Ai, Qixin Zhu, Feng Wang, Qi Su, Bing Xu
Publikováno v:
Chinese Journal of Mechanical Engineering, Vol 37, Iss 1, Pp 1-14 (2024)
Abstract Hydraulic actuated quadruped robots have bright application prospects and significant research values in unmanned area investigation, disaster rescue and other scenarios, due to the advantages of high payload and high power to weight ratio.
Externí odkaz:
https://doaj.org/article/26f1b686a7014f1fa66ea6c505f1ae07
Publikováno v:
Frontiers in Neurology, Vol 15 (2024)
BackgroundTRIM8-related neuro-renal syndrome (NRS), caused by pathogenic variants of the TRIM8 gene, is characterized by epilepsy, developmental delay (DD) and renal disorders. The severity of the neurological effects as well as the presence of renal
Externí odkaz:
https://doaj.org/article/8e89c2c864e44117baf61b2218c9a853
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 18 (2024)
Epilepsy is a common neurological disorder that affects approximately 10.5 million children worldwide. Approximately 33% of affected patients exhibit resistance to all available antiseizure medications, but the underlying mechanisms are unknown and t
Externí odkaz:
https://doaj.org/article/47713fb2f80f476fb51ac94a78269d83
Publikováno v:
Food and Energy Security, Vol 13, Iss 3, Pp n/a-n/a (2024)
Abstract Continuous cultivation of faba beans often results in a high occurrence of Fusarium wilt. Nevertheless, this issue can be successfully managed through wheat‐faba bean intercropping. Our objective is to elucidate the function of non‐host
Externí odkaz:
https://doaj.org/article/e1b0ed93e3d74452a88d619c40843c0c
Publikováno v:
Frontiers in Neurology, Vol 15 (2024)
ObjectivesThis study aimed to investigate the clinical, radiological, and genetic features of POLR3-related leukodystrophy caused by mutations in POLR3A or POLR1C.MethodsFourteen Chinese patients with POLR3-related leukodystrophy were enrolled in thi
Externí odkaz:
https://doaj.org/article/f22aaecd04294373a7a6aa18c76d23cc
Publikováno v:
Epilepsia Open, Vol 8, Iss 2, Pp 268-277 (2023)
Abstract This systematic review and meta‐analysis aimed to evaluate the efficacy of vigabatrin (VGB) in treating infantile epileptic spasms syndrome (IESS). Databases of PubMed, Embase, Web of Science, MEDLINE, and Cochrane Library were systematica
Externí odkaz:
https://doaj.org/article/f05b19e2f8c4456b86ed321eb532d6e2
Autor:
Xuan Zhang, Hongjuan Lu, Hanran Yang, Yichen Ji, Huixin Liu, Wenjian Liu, Jiayi Li, Zhixian Yang, Wei Sun
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Structural rearrangements of chromosome 4p gives rise to a group of rare genomic disorders that mainly result in two different clinical entities: Wolf-Hirschhorn syndrome (WHS) and partial 4p trisomy. The severity of the phenotype depends on the size
Externí odkaz:
https://doaj.org/article/c1a1d895c4674dd68e2c571ea21ee03f
Publikováno v:
Acta Epileptologica, Vol 4, Iss 1, Pp 1-5 (2022)
Abstract Background Landau-Kleffner syndrome (LKS) is an acquired aphasia and electroencephalogram (EEG) abnormalities mainly in temporoparietal areas. SLC26A4 mutations can cause hearing loss associated with enlarged vestibular aqueduct (EVA). Case
Externí odkaz:
https://doaj.org/article/c9a86ccb21474a9db634dbbe606121ea
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
ObjectivesTo investigate neonatal electroencephalography (EEG) background activity and electrographic seizures in patients in the pediatric intensive care unit (PICU) who underwent bedside video-electroencephalography (vEEG) monitoring.MethodsA total
Externí odkaz:
https://doaj.org/article/8ffc17aafd4b4763a17ed070606c52ae
Autor:
Yi Chen, Xiaoxu Yang, Jiaoyang Chen, Xiaoling Yang, Ying Yang, Aijie Liu, Xiaoli Zhang, Wenjuan Wu, Dan Sun, Zhixian Yang, Yuwu Jiang, Yuehua Zhang
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
ObjectiveTo analyze the genotypes and phenotypes of mosaic male patients with PCDH19-related epilepsy (PCDH19-RE) and explore the correlation between genotype, variant allele frequency (VAF), and phenotypic severity.MethodsClinical data and periphera
Externí odkaz:
https://doaj.org/article/f89026c6f89b4d4797cfdd5d642dcf46